# The impact of rifampin on the efficacy of implant retention and prosthesis removal in staphylococcal periprosthetic joint infection

**Authors:** Canhong Zhang, Juncheng Li, Lan Lin, Mingzhong Liu, Yang Chen, Yuanqing Cai, Jiexin Huang, Zida Huang, Chaofan Zhang, Wenming Zhang, Xinyu Fang, Wenbo Li

PMC · DOI: 10.3389/fcimb.2025.1587436 · Frontiers in Cellular and Infection Microbiology · 2025-07-16

## TL;DR

This study found that adding rifampin to standard treatment for staphylococcal joint infections did not improve outcomes but increased side effects.

## Contribution

The study provides new evidence that rifampin does not significantly improve treatment outcomes for staphylococcal prosthetic joint infections.

## Key findings

- Rifampin did not significantly improve remission rates compared to standard treatment.
- Rifampin increased the risk of drug-related adverse events.
- Diabetes and smoking were significant risk factors for treatment failure, but rifampin was not.

## Abstract

The purpose of this study was to evaluate the impact of adjunctive rifampicin therapy on the outcomes of prosthesis retention versus removal in patients with staphylococcal prosthetic joint infection (PJI) undergoing antibacterial treatment.

A retrospective study was conducted on 227 patients diagnosed with Staphylococcal PJI from March 2014 to September 2023 who underwent debridement, antibiotics, and implant retention (DAIR) or explantation and revision surgery. Based on antimicrobial susceptibility testing, we used an effective baseline antibiotic regimen. We defined the combination of this regimen with rifampicin as the “rifampicin treatment group” and the regimen without rifampicin as the “non-rifampicin treatment group”.

A total of 79 patients were included in the rifampin treatment group and 148 in the non-rifampin treatment group. There was no significant difference in the remission rate of PJI between the rifampin treatment group and the non-rifampin treatment group (79.75% vs 73.65%, p = 0.083). Additionally, Kaplan-Meier survival curve analysis showed no statistically significant difference between the two groups (p = 0.509). However, the incidence of drug-related adverse events was significantly higher in the rifampin treatment group compared to the non-rifampin treatment group (31.65% vs 8.78%, p < 0.001). There were no significant difference in treatment success rates between the use and non-use of rifampin in DAIR, one-stage revision, or two-stage revision, as well as in hip or knee joints. Binary logistic regression analysis identified diabetes and active smoking as independent significant risk factors for treatment failure, while rifampin was not an independent risk factor affecting the outcome.

The study has not demonstrated that the standard antibiotic regimen combined with rifampin has a significant effect on the efficacy of retaining or removing prostheses in staphylococcal PJI, but rather increases drug-related adverse events. Standard surgical procedures, accurate pathogen diagnosis, and treatment are particularly crucial in the management of PJI.

## Linked entities

- **Chemicals:** rifampin (PubChem CID 135398735)
- **Diseases:** diabetes (MONDO:0005015)

## Full-text entities

- **Genes:** CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}
- **Diseases:** arrhythmias (MESH:D001145), MRSA (MESH:D013203), end-stage joint diseases (MESH:D007676), hypotension (MESH:D007022), PJI (MESH:D007239), infectious disease (MESH:D003141), hip and (MESH:D025981), smoking (MESH:D015208), allergies (MESH:D004342), necrotic (MESH:D009336), staphylococcal (MESH:D011023), diabetes (MESH:D003920), Musculoskeletal Infection (MESH:D009140), bone loss (MESH:D001847), CoNS (MESH:D064726), MR (MESH:D008944), gastrointestinal symptoms (MESH:D012817), autoimmune disease (MESH:D001327), MS (MESH:D009103), bacterial infections (MESH:D001424)
- **Chemicals:** methicillin (MESH:D008712), polyethylene (MESH:D020959), vancomycin (MESH:D014640), phenol (MESH:D019800), Rifampicin (MESH:D012293), saline (MESH:D012965), DAIR (-), creatinine (MESH:D003404), meropenem (MESH:D000077731), cefazolin (MESH:D002437), fluoroquinolone (MESH:D024841), povidone-iodine (MESH:D011206), cephalosporins (MESH:D002511)
- **Species:** Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Staphylococcus aureus (species) [taxon 1280], Homo sapiens (human, species) [taxon 9606], Staphylococcus epidermidis (species) [taxon 1282]

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## Figures

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## References

43 references — full list in the complete paper: https://tomesphere.com/paper/PMC12307336/full.md

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Source: https://tomesphere.com/paper/PMC12307336